A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239934



Internal ID20806974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14534062..14534997hg38UCSC Ensembl
chr16:14627919..14628854hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38936
hg19936
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583254
Supporting Variants
Samples
Known GenesPARN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239934
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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